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2,6-Dichlorophenol is a compound with formula C 6 H 3 Cl 2 OH. It is one of the six isomers of dichlorophenol. It is a colorless solid. Its pK a is 6.78, which is about 100x more acidic than 2-chlorophenol (8.52) and 1000x more acidic than phenol itself (9.95). [3]
10466–65–6 KRuO 4: potassium perruthenate: 10378–50–4 KSCN: potassium thiocyanate: 333–20–0 KVO 3: potassium metavanadate: 13769–43–2 K 2 CO 3: potassium carbonate: 584–08–7 K 2 C 2 O 4: potassium oxalate: 583–52–8 K 2 C 4 H 6 O 6: potassium tartrate: 921–53–9 K 2 C 6 H 8 O 4: potassium adipate: 19147–16–1 K 2 ...
For homopolymerization of ECC 1.5 to 3 wt. % of an initiator are added. Above 3 wt% initiator no further acceleration was found, increasing proportions of initiators, however, increase the brittleness of the formed thermoset. After a photopolymerization usually still a thermal post-curing is necessary for a complete reaction. [5]
C 5 H 6 N 2 O 2: thymine: 65-71-4 C 5 H 6 O: cyclopentenone: C 5 H 6 O 5: α-Ketoglutaric acid: 328-50-7 C 5 H 7 N 3: 3,4-diaminopyridine: 54-96-6 C 5 H 8 O 2: gamma-Valerolactone: C 5 H 9 NO 3-Dimethylaminoacrolein: 927-63-9 C 5 H 9 NO 2: allylglycine: C 5 H 9 NO 2: proline Pro: 147-85-3 C 5 H 9 NO 4: glutamic acid Glu: 56-86-0 C 5 H 10 ...
C 6 H 10 O 8: saccharic acid: 87-73-0 C 6 H 10 S 2: diallyl disulfide: 2179-57-9 C 6 H 10 S 3: diallyl trisulfide: 2050-87-5 C 6 H 10 S 4: diallyl tetrasulfide: 2444-49-7 C 6 H 11: cyclohexyl radical: 3170-58-9 C 6 H 11 BrHg: cyclohexyl mercuric bromide: 10192-55-9 C 6 H 11 BrN 2 O 2: bromisovalum: 496-67-3 C 6 H 11 BrO 2: butyl bromoacetate ...
A study of house dust in the U.S. found that over 96% of samples collected between 2002 and 2007 contained TDCPP at an average concentration of over 1.8 ppm, while the highest was over 56 ppm. [5] TDCPP was also detected in 99% of dust samples collected in 2009 in the Boston area from offices, homes, and vehicles.
Like other hydroxylamines it will react with aldehydes to form nitrones, illustrative is the condensation with benzaldehyde to form diphenylnitrone, a well-known 1,3-dipolar compound: [4] C 6 H 5 NHOH + C 6 H 5 CHO → C 6 H 5 N(O)=CHC 6 H 5 + H 2 O. Phenylhydroxylamine is attacked by NO + sources to give cupferron: [5] C 6 H 5 NHOH + C 4 H 9 ...
1-(2-Chloro-N-methylbenzimidoyl)cyclopentanol, sometimes misleadingly referred to as hydroxylimine hydrochloride, is a chemical compound which is the final intermediate in the synthesis of ketamine, an anaesthetic drug which is also subject to recreational abuse.